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Analysis of MicroRNA Expression in Embryonic Developmental Toxicity Induced by MC-RR
As cynobacterial blooms frequently occur in fresh waters throughout the world, microcystins (MCs) have caused serious damage to both wildlife and human health. MCs are known to have developmental toxicity, however, the possible molecular mechanism is largely unknown. This is the first toxicological...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3146480/ https://www.ncbi.nlm.nih.gov/pubmed/21829477 http://dx.doi.org/10.1371/journal.pone.0022676 |
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author | Zhao, Yanyan Xiong, Qian Xie, Ping |
author_facet | Zhao, Yanyan Xiong, Qian Xie, Ping |
author_sort | Zhao, Yanyan |
collection | PubMed |
description | As cynobacterial blooms frequently occur in fresh waters throughout the world, microcystins (MCs) have caused serious damage to both wildlife and human health. MCs are known to have developmental toxicity, however, the possible molecular mechanism is largely unknown. This is the first toxicological study to integrate post-transcriptomic, proteomic and bioinformatics analysis to explore molecular mechanisms for developmental toxicity of MCs in zebrafish. After being microinjected directly into embryos, MC-RR dose-dependently decreased survival rates and increased malformation rates of embryos, causing various embryo abnormalities including loss of vascular integrity and hemorrhage. Expressions of 31 microRNAs (miRNAs) and 78 proteins were significantly affected at 72 hours post-fertilisation (hpf). Expressions of miR-430 and miR-125 families were also significantly changed. The altered expressions of miR-31 and miR-126 were likely responsible for the loss of vascular integrity. MC-RR significantly reduced the expressions of a number of proteins involved in energy metabolism, cell division, protein synthesis, cytoskeleton maintenance, response to stress and DNA replication. Bioinformatics analysis shows that several aberrantly expressed miRNAs and proteins (involved in various molecular pathways) were predicted to be potential MC-responsive miRNA-target pairs, and that their aberrant expressions should be the possible molecular mechanisms for the various developmental defects caused by MC-RR. |
format | Online Article Text |
id | pubmed-3146480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31464802011-08-09 Analysis of MicroRNA Expression in Embryonic Developmental Toxicity Induced by MC-RR Zhao, Yanyan Xiong, Qian Xie, Ping PLoS One Research Article As cynobacterial blooms frequently occur in fresh waters throughout the world, microcystins (MCs) have caused serious damage to both wildlife and human health. MCs are known to have developmental toxicity, however, the possible molecular mechanism is largely unknown. This is the first toxicological study to integrate post-transcriptomic, proteomic and bioinformatics analysis to explore molecular mechanisms for developmental toxicity of MCs in zebrafish. After being microinjected directly into embryos, MC-RR dose-dependently decreased survival rates and increased malformation rates of embryos, causing various embryo abnormalities including loss of vascular integrity and hemorrhage. Expressions of 31 microRNAs (miRNAs) and 78 proteins were significantly affected at 72 hours post-fertilisation (hpf). Expressions of miR-430 and miR-125 families were also significantly changed. The altered expressions of miR-31 and miR-126 were likely responsible for the loss of vascular integrity. MC-RR significantly reduced the expressions of a number of proteins involved in energy metabolism, cell division, protein synthesis, cytoskeleton maintenance, response to stress and DNA replication. Bioinformatics analysis shows that several aberrantly expressed miRNAs and proteins (involved in various molecular pathways) were predicted to be potential MC-responsive miRNA-target pairs, and that their aberrant expressions should be the possible molecular mechanisms for the various developmental defects caused by MC-RR. Public Library of Science 2011-07-29 /pmc/articles/PMC3146480/ /pubmed/21829477 http://dx.doi.org/10.1371/journal.pone.0022676 Text en Zhao et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zhao, Yanyan Xiong, Qian Xie, Ping Analysis of MicroRNA Expression in Embryonic Developmental Toxicity Induced by MC-RR |
title | Analysis of MicroRNA Expression in Embryonic Developmental Toxicity Induced by MC-RR |
title_full | Analysis of MicroRNA Expression in Embryonic Developmental Toxicity Induced by MC-RR |
title_fullStr | Analysis of MicroRNA Expression in Embryonic Developmental Toxicity Induced by MC-RR |
title_full_unstemmed | Analysis of MicroRNA Expression in Embryonic Developmental Toxicity Induced by MC-RR |
title_short | Analysis of MicroRNA Expression in Embryonic Developmental Toxicity Induced by MC-RR |
title_sort | analysis of microrna expression in embryonic developmental toxicity induced by mc-rr |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3146480/ https://www.ncbi.nlm.nih.gov/pubmed/21829477 http://dx.doi.org/10.1371/journal.pone.0022676 |
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